ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.2529T>C (p.Asn843=)

dbSNP: rs1330790224
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001487853 SCV001692350 likely benign Familial hemiplegic migraine 2020-09-01 criteria provided, single submitter clinical testing

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